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T22992ML 10302 hydrochlorideML 10302 hydrochloride
ML 10302 hydrochloride is a specific agonist 5-HT4 and binds 5-HT receptors with Kis of 1.07 nM and 782 nM for 5-HT4 and 5-HT3.
价 格：￥电议型 号：T22992产 地：中国大陆
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T7366NGI-1ML 414,inhibit,Inhibitor,NGI 1,ML-414,NGI-1,Virus Protease,NGI1
NGI-1 is a a cell-permeable inhibitor of oligosaccharyltransferase (OST).can effectively reduce virus infectivity without affecting cell viability.
价 格：￥电议型 号：T7366产 地：中国大陆
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TP1890L1MLCK inhibitor peptide 18 acetateMLCK inhibitor peptide 18 acetate
MLCK inhibitor peptide 18 acetate is a selective competitive inhibitor of myosin light chain kinase (IC50 = 50 nM). Displays 4000-fold selectivity over CaM kinase II and does not inhibit PKA. Cell permeable.
价 格：￥电议型 号：TP1890L1产 地：中国大陆
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T7138FB23-2FB23 2,AML,Apoptosis,leukemia,acute,anti-proliferation,Inhibitor,FB232,m6A,myeloid,mRNA,inhibi
FB23-2 is a potent and selective mRNA N6-methyladenosine (m6A) demethylase FTO inhibitor(IC50 : 2.6 μM).
价 格：￥电议型 号：T7138产 地：中国大陆
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T64338AKI603AKI603,Aurora Kinase,chronic,CML,leukemia,myeloid,inhibit,imatinib-resistant,Inhibitor
AKI603 is a novel small molecule inhibitor of Aurora kinase A (AurA)(IC50 = 12.3 nM). AKI603 is developed to overcome resistance mediated by BCR-ABL-T315I mutation. AKI603 exhibits strong anti-proliferative activity in leukemic cells[1][2].
价 格：￥电议型 号：T64338产 地：中国大陆
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T6593ML324ML-324,Jumonji,periodontal,Cytomegalovirus,ML324,inhibit,simplex,CMV,Inhibitor,Herpes simplex v
ML324(IC50=920 nM) is a specific inhibitor of jumonji histone demethylase (JMJD2).
价 格：￥电议型 号：T6593产 地：中国大陆
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T8994ML-?226MAGL,inhibit,ML-?226,Inhibitor,ML?226,ML ?226,Monoacylglycerol lipase
ML226 is a α/β hydrolase domain-containing protein 11 (ABHD11) inhibitor that inhibits ABHD11 in vitro and in situ.
价 格：￥电议型 号：T8994产 地：中国大陆
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TP1915Boc-MLFBoc MLF,BocMLF
Antagonist of formyl peptide receptor 1 (FPR1). Reduces superoxide production induced by fMLF with an EC50 of 0.63 μM. Almost completely blocks fMLF-stimulated primary granule exocytosis.
价 格：￥电议型 号：TP1915产 地：中国大陆
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T6592ML133 hydrochloridePotassium Channel,KcsA,Inhibitor,inhibit,ML 133,ML-133 hydrochloride,ML133 hydroc
ML133 HCl is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 μM (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 and weak activity for Kir4.1 and Kir7.1.
价 格：￥电议型 号：T6592产 地：中国大陆
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T8571ML-184ML184,ML-184,inhibit,CID 2440433,ML 184,G protein-coupled receptor 55,CID-2440433,Inhibitor,GP
ML-184 is a potent synthetic agonist of GPR55 with EC50 of 0.26 μM.
价 格：￥电议型 号：T8571产 地：中国大陆
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T8397Ixazomib citrateProteasome,MLN 9708,Ixazomib,Inhibitor,Ixazomib citrate,MLN-9708,Autophagy,inhibit
Ixazomib citrate is a prodrug of Ixazomib (MMLN-2238). MLN9708 is an orally bioavailable second generation proteasome inhibitor (IC50 of 3.4 nM ) with potential antineoplastic activity.
价 格：￥电议型 号：T8397产 地：中国大陆
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T7648HA-100protein,PKC,Rho-associated kinase,ROCK,kinase,PKG,HA100,inhibit,Inhibitor,Myosin,HA 100,MLCK,H
HA-100 is an inhibitor of protein kinase
价 格：￥电议型 号：T7648产 地：中国大陆
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T37587ML 209ML 209,ML209
ML-209 is an antagonist of retinoic acid receptor-related orphan receptor γt (RORγt; IC50= 1.1 μM in a reporter assay).1It inhibits RORγt-induced transcription in HEK293T cells expressing the human receptor (IC50= 300 nM). ML-209 inhibits RORγt-dependent differentiation of isolated na?ve cord blood human CD4+T cells into Th17 T helper cells.
价 格：￥电议型 号：T37587产 地：中国大陆
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T6591Nodinitib-1Nodinitib1,CID1088438,Inhibitor,NOD-like Receptor (NLR),Nodinitib 1,ML-130,ML 130,Nodinit
Nodinitib-1 is a potent and selective NOD1 inhibitor with an IC50 of 0.56 μM.
价 格：￥电议型 号：T6591产 地：中国大陆
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T8986ML198inhibit,ML198,ML-198,ML 198,GCase modulator,Inhibitor,Non-inhibitory chaperone,Gaucher disease,
ML198 is a novel activator and non-inhibitory chaperone of glucocerebrosidase. ML198 serves as a starting point to develop a novel approach towards small molecule treatment for patients suffering from Gaucher disease.
价 格：￥电议型 号：T8986产 地：中国大陆
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T9399Menin-MLL inhibitor 20Epigenetic Reader Domain,mixed-lineage,MeninMLL inhibitor 20,irreversible,leuk
Menin-MLL inhibitor 20 is an irreversible inhibitor of menin-MLL interaction with antitumor activities (WO2020142557A1, compound 6).
价 格：￥电议型 号：T9399产 地：中国大陆
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T8514LML134inhibit,LML134,LML 134,Inhibitor,Histamine Receptor
LML-134 is an inverse agonist of Histamine 3 receptor (H3R)(hH3R cAMP and hH3R bdg with Kis of 0.3 nM and 12 nM).
价 格：￥电议型 号：T8514产 地：中国大陆
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T16766Ro 08-2750growth,MSI,Ro 082750,p75NTR,TRKA,RNA-binding,Nerve,NGF,Inhibitor,leukemia,Apoptosis,AML,Ro
Ro 08-2750 is a non-peptide and reversible nerve growth factor (NGF) inhibitor which binds to NGF, and with an IC50 of ~ 1 ?M. Ro 08-2750 is a selective MSI RNA-binding activity inhibitor, with an IC50 of 2.7 μM. Ro 08-2750 inhibits NGF binding to p75NTR selectively over TRKA.
价 格：￥电议型 号：T16766产 地：中国大陆
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T6411BiapenemL627,inhibit,L-627,CLI86815,LJC10627,Bacterial,LJC-10627,Antibiotic,CLI-86815,Biapenem,Inhib
Biapenem is a 1-beta-methylcarbapenem antibiotic with a wide range of antibacterial activity. Biapenem has similar antibacterial activity to that of imipenem, but is more stable against human renal dehydropeptidase-I and with less neurotoxicity.
价 格：￥电议型 号：T6411产 地：中国大陆
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TP2320Pramlintide acetate(151126-32-8 free base)Pramlintide acetate(151126 32 8 free base),Pramlintide ace
Pramlintide acetate is a polypeptide analogue of human amylin. Pramlintide acetate, an antidiabetic agent, is antineoplastic in colorectal cancer.
价 格：￥电议型 号：TP2320产 地：中国大陆
